Classifications

• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07J—STEROIDS
  • C07J5/00—Normal steroids containing carbon, hydrogen, halogen or oxygen, substituted in position 17 beta by a chain of two carbon atoms, e.g. pregnane and substituted in position 21 by only one singly bound oxygen atom, i.e. only one oxygen bound to position 21 by a single bond
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07J—STEROIDS
  • C07J71/00—Steroids in which the cyclopenta(a)hydrophenanthrene skeleton is condensed with a heterocyclic ring
  • C07J71/0005—Oxygen-containing hetero ring
  • C07J71/0026—Oxygen-containing hetero ring cyclic ketals
  • C07J71/0031—Oxygen-containing hetero ring cyclic ketals at positions 16, 17
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]

Definitions

• the present invention relates to novel, pharmacologically active compounds, a process for their preparation including the separation of the obtained stereoisomeric mixture into its separate components (diastereoisomers).
• the invention also relates to pharmaceutical compositions containing the compounds and to methods of treatment of inflammatory conditions with these compounds.
• the object of the invention is to provide a steroid compound which possesses a combination of high anti-inflammatory potency on the place of application and low glucocorticoid systemic effects.
• glucocorticoids can be used for topical treatment of inflammatory and allergic conditions in the skin and respiratory airways and for injection therapy at diseases of the joints.
• the Swedish Pat. No. 378 110 discloses anti-inflammatory active stereoisomeric components of a stereoisomeric mixture of a steroid having the general formula: ##STR2## wherein the 1,2 and 4,5-positions are saturated or a double bond present in at least one of said two positions, X 1 and X 2 are the same or different and selected among hydrogen and fluorine, Z is hydroxyl or esterified hydroxyl and R is an alkyl group with straight or branched hydrocarbon chains having 1-10 carbon atoms.
• the present invention is based on the observation that certain unsymmetrical 16,17-acetals of 16 ⁇ -hydroxycortisol possess a high anti-inflammatory potency on the place of application in combination with low glucocorticoid systemic effects.
• the compounds of the invention can be used for the treatment and control of severe inflammatory conditions.
• the compounds of the invention are characterized by the formula ##STR4## wherein A is n-propyl or n-butyl and Z is hydroxyl or hydroxyl esterified with a fatty acid with a straight or branched hydrocarbon chain having 1-5 carbon atoms.
• Diastereoisomers like II and III, in which the configuration differs only at one (C-22) out of several asymmetric carbon atoms are denoted epimers.
• the compounds of the invention are prepared by reaction of 16 ⁇ -hydroxycortisol of the formula ##STR6## with an aldehyde of the formula
• A is n-propyl or n-butyl
• B 1 to B 6 are the same or different and each representing hydrogen or an alkyl group with straight or branched hydrocarbon chains having 1-10 carbon atoms, selected among methyl, ethyl, propyl, iso-propyl, butyl, iso-butyl, tert-butyl, pentyl, hexyl, heptyl, octyl, nonyl or decyl, e.g.
• the obtained product is esterified.
• the esterification is performed with a fatty acid with a straight or branched hydrocarbon chain having 1-5 carbon atoms.
• the fatty acid can for instance be acetic acid, butyric acid or trimethyl acetic acid.
• the reaction between 16 ⁇ -hydroxycortisol and the aldehyde or the acetal is suitably carried out by adding the steroid to a solution of the aldehyde or the acetal together with an acid catalyst e.g. perchloric acid, p-toluene sulphonic acid, hydrochloric acid etc. in dioxane or equivalent solvents, the reaction mixture being then taken up in methylene chloride and neutralized.
• an acid catalyst e.g. perchloric acid, p-toluene sulphonic acid, hydrochloric acid etc. in dioxane or equivalent solvents
• the crude steroid acetal derivative formed which is composed of a mixture of the 22R- and 22S-epimers, is after isolation purified by chromatography on a suitable material, for instance crosslinked dextran gels of Sephadex® LH-type with suitable solvents as eluants, e.g. halogenated hydrocarbons, ethers, esters such as ethyl acetate or acetonitrile.
• suitable solvents as eluants, e.g. halogenated hydrocarbons, ethers, esters such as ethyl acetate or acetonitrile.
• the free acid its halide or anhydride may be used in the esterification reaction.
• the individual R and S epimers which are formed at the reaction, possess practically identical solubility characteristics. Accordingly, they have turned out to be impossible to separate and isolate from the epimeric mixture by conventional methods for resolution of stereoisomers, e.g. fractionated crystallization.
• the process according to the invention consists in subjecting stereoisomeric mixtures according to the formula (I) above to column chromatography, the epimers R and S being separated in view of different mobility on the stationary phase, why they can be separately recovered.
• the chromatography may be carried out for instance on cross-linked dextran gels of the type Sephadex® LH, e.g. Sephadex® LH-20 in combination with a suitable organic solvent as eluting agent.
• Sephadex® LH-20 prepared by Pharmacia Fine Chemicals AB, Uppsala, Sweden, is a bead-formed hydroxypropylated dextran gel wherein the dextran chain are cross-linked to give a three-dimensional polysaccharide network.
• eluting agent a mixture of n-heptane-chloroform-ethanol in the proportions 0-50:50-100:10-1 has successfully been used, preferably a 20:20:1 mixture.
• the epimers R and S with the general formulas (II) and (III) respectively above, wherein Z is hydroxyl can also be obtained from a stereoisomeric mixture with the general formula (I) above, wherein Z is hydroxyl esterified with a fatty acid, after resolution by chromatography on Sephadex® LH-20 together with a suitable solvent or mixture of solvents, e.g. n-heptane-chloroform-ethanol in the proportions 0-50:50-100:10-1, preferably 20:20:1, as mobile phase.
• a suitable solvent or mixture of solvents e.g. n-heptane-chloroform-ethanol in the proportions 0-50:50-100:10-1, preferably 20:20:1, as mobile phase.
• the separated and isolated epimers R and S with the general formula (II) and (III) respectively above, wherein Z is hydroxyl esterified with a fatty acid may be, if so desired, submitted to base catalyzed hydrolysis, with hydroxides, carbonates or hydrogen carbonates of alkaline metals, e.g. sodium or potassium hydroxide, sodium or potassium carbonate or sodium or potassium hydrogen carbonate, to give the epimers R and S, wherein Z is hydroxyl.
• alkaline metals e.g. sodium or potassium hydroxide, sodium or potassium carbonate or sodium or potassium hydrogen carbonate
• the compounds of the invention may be used for different modes of local administration dependent on the site of inflammation, e.g. percutaneously, parenterally or for local administration in the respiratory airways by inhalation.
• An important aim of the formulation design is to reach optimal bioavailability of the active steroid ingredient. For percutaneous formulations this is advantageously achieved if the steroid is dissolved with a high thermodynamic activity in the vehicle. This is attained by using a suitable system of solvents comprising suitable glycols, such as propylene glycol or 1,3-butanediol either as such or in combination with water.
• the percutaneous compositions can be an ointment, an oil in water cream, a water in oil cream or a lotion.
• the system comprising the dissolved active component can make up the disperse phase as well as the continuous one.
• the steroid can also exist in the above compositions as a micronized, solid substance.
• Compressed aerosols for steroids are intended for oral or nasal inhalation.
• the aerosol system is designed in such a way that each delivered dosage contains 100-1000 ⁇ g, preferably 20-250 ⁇ g of the active steroid.
• the most active steroids are administered in the lower part of the dosage range.
• the micronized steroid consists of particles substantially smaller than 5 ⁇ m, which are suspended in a propellant gas mixture with the assistance of a dispersant, such as sorbitan trioleate, oleinic acid, lecithin or sodium salt of dioctylsulphosuccinic acid.
• the product from the first fraction (16.5 mg) was identified with the aid of 1 H-NMR and mass spectrometry to be the 22S-epimer and the product from the latter fraction (13.0 mg) in the same way as the 22R-epimer.
• the epimers had the following properties.
• the purity of the epimers was determined by HPLC-analysis to be 99.7% for the S-epimer and 95.0% for the R-epimer. 4% of the impurities of the R-epimer consists of epimer S.
• the purity of the epimers was determined by HPLC-analysis to be 97.3% (contains 2.1% of the R-epimer) for the S-epimer and 97.9% (contains 0.5% of the S-epimer) for the R-epimer.
• the epimers had the following properties.
• the purity of the epimers was determined by HPLC-analysis to be 97.5% (contains 1.3% of the R-epimer) for the S-epimer and 97.1% (contains 1.2% of the S-epimer) for the R-epimer.
• the epimers had the following properties.
• the following non-limitative examples illustrate formulations intended for different topical forms of administration.
• the amount of active steroid in the percutaneous formulations are ordinarily 0.001-0.2% (w/w), preferably 0.01-0.1% (w/w).
• All steroids according to the present invention are physiologically active compounds.
• the glucocorticoid properties of the compounds have been compared with those of budesonide (16 ⁇ ,17 ⁇ -[22R,S]-propylmethylenedioxypregna-1,4-diene-11 ⁇ ,21-diol-3,20-dione), as this compound is one of the glucocorticoids which today has reached most far towards the desired combination of local and systemic effects (Thalen and Brattsand, Arzneim.-Forsch. 29, 1687-1690 (1979)).
• the topical anti-inflammatory activity has been investigated as the potency to prevent ear edema in rats according to the following procedure.
• the potency of the compounds to induce systemic glucocorticoid effects has been investigated by s.c. injections as no systemic effects are attained with the dose levels used in the above mentioned topical test.
• 0.5 ml steroid preparation was injected into rats of the same sex and weight as above.
• At least 5 doses of each test compound were injected within the dose range 20-1280 ⁇ g/rat with 4 animals per dose.
• the body weight gain of the animals was determined during the first two days after injection and the thymus weight after two further days as these time intervals are the optimal ones for determination of the respective systemic effect.
• the relative potency of the compounds was calculated with linear regression analysis in relation to the reference substance budesonide.
• Table 1 The results of the tests of the glucocorticoids of the invention in accordance with the procedure given above are shown in Table 1.
• the new compounds are 3-20 times less potent than budesonide to induce non-desirable systemic glucocorticoid effects.
• the new compounds also have 5-10 times higher anti-inflammatory potency than the previously known 16 ⁇ ,17 ⁇ -[22R]-methylmethylenedioxy-4-pregnene-11 ⁇ ,21-diol-3,20-dione (Swedish patent no 378 110) while they are equally potent when comparing the systemic glucocorticoid activities.

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• Organic Chemistry (AREA)
• Chemical & Material Sciences (AREA)
• Health & Medical Sciences (AREA)
• General Health & Medical Sciences (AREA)
• Medicinal Chemistry (AREA)
• Chemical Kinetics & Catalysis (AREA)
• Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
• Rheumatology (AREA)
• Pharmacology & Pharmacy (AREA)
• Life Sciences & Earth Sciences (AREA)
• Animal Behavior & Ethology (AREA)
• Pain & Pain Management (AREA)
• Public Health (AREA)
• Veterinary Medicine (AREA)
• General Chemical & Material Sciences (AREA)
• Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
• Steroid Compounds (AREA)
• Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
• Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
• Dental Preparations (AREA)
• Saccharide Compounds (AREA)
• Investigating Or Analysing Biological Materials (AREA)
• Medicines Containing Plant Substances (AREA)
• Polysaccharides And Polysaccharide Derivatives (AREA)
• Treating Waste Gases (AREA)
• Peptides Or Proteins (AREA)
• Diaphragms For Electromechanical Transducers (AREA)

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Publications (1)

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Country Status (26)

Cited By (8)

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Citations (8)

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• 1980
  • 1980-12-04 SE SE8008524A patent/SE8008524L/xx not_active Application Discontinuation
• 1981
  • 1981-11-10 ZA ZA817772A patent/ZA817772B/xx unknown
  • 1981-11-17 US US06/322,592 patent/US4404200A/en not_active Expired - Lifetime
  • 1981-11-18 CY CY141381A patent/CY1413A/xx unknown
  • 1981-11-18 EP EP81850219A patent/EP0054010B1/de not_active Expired
  • 1981-11-18 DE DE8181850219T patent/DE3169108D1/de not_active Expired
  • 1981-11-18 AT AT81850219T patent/ATE11920T1/de not_active IP Right Cessation
  • 1981-11-23 CA CA000390673A patent/CA1183835A/en not_active Expired
  • 1981-11-27 FI FI813807A patent/FI70582C/fi not_active IP Right Cessation
  • 1981-12-01 NO NO814098A patent/NO158508C/no unknown
  • 1981-12-02 DD DD81235333A patent/DD202034A5/de unknown
  • 1981-12-02 IE IE2827/81A patent/IE51923B1/en unknown
  • 1981-12-02 GR GR66673A patent/GR76919B/el unknown
  • 1981-12-02 AU AU78169/81A patent/AU546379B2/en not_active Ceased
  • 1981-12-02 PH PH26563A patent/PH17826A/en unknown
  • 1981-12-02 NZ NZ199141A patent/NZ199141A/en unknown
  • 1981-12-03 SU SU813362002A patent/SU1156600A3/ru active
  • 1981-12-03 ES ES507670A patent/ES8306164A1/es not_active Expired
  • 1981-12-03 HU HU813638A patent/HU183717B/hu not_active IP Right Cessation
  • 1981-12-03 PT PT74078A patent/PT74078B/pt unknown
  • 1981-12-03 JP JP56193761A patent/JPS57122100A/ja active Granted
  • 1981-12-03 CS CS818959A patent/CS229923B2/cs unknown
  • 1981-12-03 DK DK535981A patent/DK163003C/da not_active IP Right Cessation
  • 1981-12-04 KR KR1019810004728A patent/KR870001904B1/ko active
• 1986
  • 1986-12-30 MY MY139/86A patent/MY8600139A/xx unknown
• 1988
  • 1988-02-10 HK HK116/88A patent/HK11688A/xx not_active IP Right Cessation

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